• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

从人类21号染色体中分离多态性DNA片段。

Isolation of polymorphic DNA segments from human chromosome 21.

作者信息

Watkins P C, Tanzi R E, Gibbons K T, Tricoli J V, Landes G, Eddy R, Shows T B, Gusella J F

出版信息

Nucleic Acids Res. 1985 Sep 11;13(17):6075-88. doi: 10.1093/nar/13.17.6075.

DOI:10.1093/nar/13.17.6075
PMID:4047940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC321939/
Abstract

A somatic cell hybrid line containing only human chromosome 21 on a mouse background has been used as the source of DNA for construction of a recombinant phage library. Individual phages containing human inserts have been identified. Repeat-free human DNA subclones have been prepared and used to screen for restriction fragment length polymorphisms to provide genetic markers on chromosome 21. Nine independently isolated clones used as probes identified a total of 11 new RFLPs. Four of the DNA probes recovered from the library have been mapped unequivocally to chromosome 21 using a panel of somatic cell hybrid lines. A fifth probe detected an RFLP on chromosome 21 as well as sequences on other chromosomes. This set of RFLPs may now form the basis for construction of a genetic linkage map of human chromosome 21.

摘要

一种以小鼠为背景、仅包含人类21号染色体的体细胞杂交系已被用作构建重组噬菌体文库的DNA来源。已鉴定出含有人类插入片段的单个噬菌体。已制备了无重复的人类DNA亚克隆,并用于筛选限制性片段长度多态性,以提供21号染色体上的遗传标记。用作探针的9个独立分离的克隆共鉴定出11个新的RFLP。从文库中回收的4个DNA探针已使用一组体细胞杂交系明确地定位到21号染色体上。第五个探针在21号染色体以及其他染色体上检测到RFLP。这组RFLP现在可能构成构建人类21号染色体遗传连锁图谱的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc27/321939/790dd468d651/nar00311-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc27/321939/650984f80ef4/nar00311-0072-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc27/321939/790dd468d651/nar00311-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc27/321939/650984f80ef4/nar00311-0072-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc27/321939/790dd468d651/nar00311-0073-a.jpg

相似文献

1
Isolation of polymorphic DNA segments from human chromosome 21.从人类21号染色体中分离多态性DNA片段。
Nucleic Acids Res. 1985 Sep 11;13(17):6075-88. doi: 10.1093/nar/13.17.6075.
2
Isolation and characterization of DNA probes from a flow-sorted human chromosome 8 library that detect restriction fragment length polymorphism (RFLP).从一个经流式细胞分选的人类8号染色体文库中分离并鉴定出可检测限制性片段长度多态性(RFLP)的DNA探针。
Am J Hum Genet. 1986 Dec;39(6):744-50.
3
Isolation of polymorphic DNA fragments from human chromosome 4.从人类4号染色体中分离多态性DNA片段。
Nucleic Acids Res. 1987 Feb 25;15(4):1445-58. doi: 10.1093/nar/15.4.1445.
4
Isolation and regional mapping of DNA sequences unique to human chromosome 21.人类21号染色体特有的DNA序列的分离与区域定位。
Am J Hum Genet. 1987 Dec;41(6):963-78.
5
Isolation of a polymorphic DNA segment unique to human chromosome 7 by molecular cloning of hybrid cell DNA.通过杂交细胞DNA的分子克隆分离出人类7号染色体特有的多态性DNA片段。
Mol Gen Genet. 1983;190(1):143-9. doi: 10.1007/BF00330337.
6
Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction.克隆的DNA探针被定位到人类21号染色体的特定区域及其在确定不分离起源中的应用。
Nucleic Acids Res. 1985 Jun 11;13(11):4125-32. doi: 10.1093/nar/13.11.4125.
7
Isolation and characterization of DNA probes from the short arm of the human X chromosome that detect restriction fragment length polymorphisms.从人类X染色体短臂分离并鉴定可检测限制性片段长度多态性的DNA探针。
Genome. 1987 Feb;29(1):201-5. doi: 10.1139/g87-034.
8
Isolation and regional localization of a large collection (2,000) of single-copy DNA fragments on human chromosome 3 for mapping and cloning tumor suppressor genes.对大量(2000个)人类3号染色体上的单拷贝DNA片段进行分离和区域定位,用于绘制和克隆肿瘤抑制基因图谱。
Hum Genet. 1991 Apr;86(6):567-77. doi: 10.1007/BF00201543.
9
Isolation and mapping of 62 new RFLP markers on human chromosome 11.人类11号染色体上62个新的限制性片段长度多态性(RFLP)标记的分离与定位。
Am J Hum Genet. 1991 Feb;48(2):258-68.
10
Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.从人类13号染色体中分离并对揭示多态性位点的DNA片段进行区域定位。
Am J Hum Genet. 1984 Jan;36(1):10-24.

引用本文的文献

1
A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes.利用酵母人工染色体构建的人类21号染色体短臂高分辨率物理图谱。
Genome Res. 1999 Nov;9(11):1059-73. doi: 10.1101/gr.9.11.1059.
2
Random-breakage mapping method applied to human DNA sequences.应用于人类DNA序列的随机断裂映射方法。
Nucleic Acids Res. 1996 May 15;24(10):1802-8. doi: 10.1093/nar/24.10.1802.
3
Partial physical map of human chromosome 21 from fibroblast and lymphocyte DNA.来自成纤维细胞和淋巴细胞DNA的人类21号染色体的部分物理图谱。

本文引用的文献

1
The insulin gene is located on the short arm of chromosome 11 in humans.胰岛素基因位于人类第11号染色体的短臂上。
Diabetes. 1981 Mar;30(3):267-70. doi: 10.2337/diab.30.3.267.
2
Mapping the human genome, cloned genes, DNA polymorphisms, and inherited disease.绘制人类基因组图谱、克隆基因、DNA多态性及遗传性疾病研究。
Adv Hum Genet. 1982;12:341-452. doi: 10.1007/978-1-4615-8315-8_5.
3
Isolation and localization of DNA segments from specific human chromosomes.从特定人类染色体中分离和定位DNA片段。
Hum Genet. 1993 Apr;91(3):245-53. doi: 10.1007/BF00218265.
4
Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.与21号染色体部分单体相关的21个特征的分子图谱:淀粉样前体蛋白-超氧化物歧化酶1区域的累及情况
Am J Hum Genet. 1995 Jul;57(1):62-71.
5
Rapid chromosomal assignment of multiple genomic clones in tomato using primary trisomics.利用初级三体在番茄中对多个基因组克隆进行快速染色体定位。
Nucleic Acids Res. 1987 Nov 25;15(22):9339-48. doi: 10.1093/nar/15.22.9339.
6
Genesis and systematization of cardiovascular anomalies and analysis of skeletal malformations in murine trisomy 16 and 19. Two animal models for human trisomies.小鼠16号和19号染色体三体中心血管异常的发生与系统化及骨骼畸形分析。两种人类三体的动物模型。
Hum Genet. 1987 Sep;77(1):12-22. doi: 10.1007/BF00284706.
7
Regional assignment of six polymorphic DNA sequences on chromosome 21 by in situ hybridization to normal and rearranged chromosomes.
Am J Hum Genet. 1988 Apr;42(4):542-9.
8
Apparent monosomy 21 owing to a ring 21 chromosome: parental origin revealed by DNA analysis.由于21号环状染色体导致的表观21号染色体单体性:通过DNA分析揭示亲本来源
J Med Genet. 1988 Dec;25(12):851-4. doi: 10.1136/jmg.25.12.851.
9
Familial Alzheimer's disease (FAD): co-segregation between alleles at the D21S11 DNA marker and the FAD gene in a particular pedigree.家族性阿尔茨海默病(FAD):在一个特定家系中,D21S11 DNA标记的等位基因与FAD基因之间的共分离。
J Neurol. 1988 Nov;235(8):485-6. doi: 10.1007/BF00314252.
10
Submicroscopic duplication of chromosome 21 and trisomy 21 phenotype (Down syndrome).21号染色体亚显微重复与21三体综合征表型(唐氏综合征)。
Hum Genet. 1987 Jul;76(3):225-9. doi: 10.1007/BF00283612.
Proc Natl Acad Sci U S A. 1980 May;77(5):2829-33. doi: 10.1073/pnas.77.5.2829.
4
Interleukin 2 (IL2) is assigned to human chromosome 4.白细胞介素2(IL2)定位于人类第4号染色体。
Somat Cell Mol Genet. 1984 May;10(3):315-8. doi: 10.1007/BF01535253.
5
Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines.环孢菌素A在建立爱泼斯坦-巴尔病毒转化的人淋巴母细胞系中的应用。
In Vitro. 1984 Nov;20(11):856-8. doi: 10.1007/BF02619631.
6
Human immune interferon gene is located on chromosome 12.人类免疫干扰素基因位于第12号染色体上。
J Exp Med. 1983 Mar 1;157(3):1020-7. doi: 10.1084/jem.157.3.1020.
7
Human genome organization of enzyme loci and metabolic diseases.酶基因座与代谢疾病的人类基因组组织
Isozymes Curr Top Biol Med Res. 1983;10:323-39.
8
Linkage disequilibrium and evolutionary relationships of DNA variants (restriction enzyme fragment length polymorphisms) at the serum albumin locus.血清白蛋白基因座处DNA变异(限制性酶切片段长度多态性)的连锁不平衡及进化关系。
Proc Natl Acad Sci U S A. 1984 Jun;81(11):3486-90. doi: 10.1073/pnas.81.11.3486.
9
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28.X连锁视网膜色素变性与经重组DNA探针L1.28鉴定的限制性片段长度多态性之间的紧密遗传连锁。
Nature. 1984;309(5965):253-5. doi: 10.1038/309253a0.
10
A polymorphic DNA marker genetically linked to Huntington's disease.一种与亨廷顿舞蹈症基因连锁的多态性DNA标记。
Nature. 1983;306(5940):234-8. doi: 10.1038/306234a0.